FDA.reportPublic FDA data

Furosemide

Product NDC
67046-219
11-digit product format
670460219
Labeler code
67046
Product ID
67046-219_5a95bc6e-5cef-4813-e053-2a91aa0a8c35
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Contract Pharmacy Services-PA
Application
NDA018487
Marketing category
NDA
Marketing start
2017-10-02
Marketing end
0000-00-00
Substance
FUROSEMIDE
Active strength
40 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d80d3aff-3a63-4d7b-a2be-fd9388b04330Product name920250806
9061e89f-9c86-4196-b34b-886fc1673cc4Product name120140821

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67046-219-072022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-142022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-152022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-202022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-212022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-282022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-302022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg
67046-219-602022-01-28C16284748780-1d6a99b39-8290-a426-e053-dadaa90af4c2219 Furosemide 40 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67046-219-07Furosemide7 in 1 BLISTER PACKTABLET71
67046-219-14Furosemide14 in 1 BLISTER PACKTABLET141
67046-219-15Furosemide15 in 1 BLISTER PACKTABLET151
67046-219-20Furosemide20 in 1 BLISTER PACKTABLET201
67046-219-21Furosemide21 in 1 BLISTER PACKTABLET211
67046-219-28Furosemide28 in 1 BLISTER PACKTABLET281
67046-219-30Furosemide30 in 1 BLISTER PACKTABLET301
67046-219-60Furosemide60 in 1 BLISTER PACKTABLET601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67046-219FUROSEMIDE TABLET [CONTRACT PHARMACY SERVICES-PA]1Legacy NDC, 8 package rows20171003_5a95bc6e-5cee-4813-e053-2a91aa0a8c35.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313988furosemide 40 MG Oral TabletPSN5a95bc6e-5cee-4813-e053-2a91aa0a8c351
313988furosemide 40 MG Oral TabletSCD5a95bc6e-5cee-4813-e053-2a91aa0a8c351

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67046-219-07670460219077 TABLET in 1 BLISTER PACK (67046-219-07) 7 tablet2017-10-020000-00-00NoNoCurrent
67046-219-146704602191414 TABLET in 1 BLISTER PACK (67046-219-14) 14 tablet2017-10-020000-00-00NoNoCurrent
67046-219-156704602191515 TABLET in 1 BLISTER PACK (67046-219-15) 15 tablet2017-10-020000-00-00NoNoCurrent
67046-219-206704602192020 TABLET in 1 BLISTER PACK (67046-219-20) 20 tablet2017-10-020000-00-00NoNoCurrent
67046-219-216704602192121 TABLET in 1 BLISTER PACK (67046-219-21) 21 tablet2017-10-020000-00-00NoNoCurrent
67046-219-286704602192828 TABLET in 1 BLISTER PACK (67046-219-28) 28 tablet2017-10-020000-00-00NoNoCurrent
67046-219-306704602193030 TABLET in 1 BLISTER PACK (67046-219-30) 30 tablet2017-10-020000-00-00NoNoCurrent
67046-219-606704602196060 TABLET in 1 BLISTER PACK (67046-219-60) 60 tablet2017-10-020000-00-00NoNoCurrent